Award for the team headed by Prof. Maciej Kurpisz.

The Main Board of the Polish Genetics Society recognized the team headed by Prof. Maciej Kurpisz (M. Kurpisz, Marta Olszewska, Ewa Wiland) with an award for the round of publications

New publication: Primary Ciliary Dyskinesia (Kartagener Syndrome).

Witt M, Bukowy-Bieryłło Z
W: Epstein’s inborn errors of development: The molecular basis of clinical disorders of morphogenesis, Ciliary  functions: Genesis, transport, and reabsorbtion, 3rd edition, Editors: Robert P. Erickson, Anthony J. Wynshaw-Boris, Oxford Monographs on Medical Genetics, ISBN 9780199934522, 8 September 2016, str. 221-227; MNiSW-5

New publication: Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

Dawidowska M, Kosmalska M, Sędek Ł, Szczepankiewicz A, Twardoch M, Sonsala A, Szarzyńska B, Derwich K, Lejman M, Pawelec K, Obitko-Płudowska A, Pawińska-Wąsikowska K, Kwiecińska K, Kołtan A, Dyla A, Grzeszczak W, Kowalczyk JR, Szczepański T, Ziętkiewicz E, Witt M
Sci Rep. 2016 Jul 18;6:29427; IF 5.228; MNiSW 40